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Modulation of the tumorigenicity of human adenovirus-12-transformed cells by interferon.

Abstract
Human adenovirus-12-transformed cells express greatly reduced levels of the major histocompatibility complex class I antigens and are highly tumorigenic in syngeneic hosts. The finding that expression of a transfected class I gene is sufficient to abrogate their tumorigenicity underscores the importance of defining the conditions that will lead to derepression of endogenous class I genes in these cells. Brief treatment of Ad12-transformed cells with interferon results in the rapid but transient expression of class I antigens, and these interferon-treated cells have significantly reduced tumorigenicity in immunocompetent hosts. We have further demonstrated that subcutaneous administration of interferon, subsequent to the introduction of a tumorigenic dose of Ad12-transformed cells, results in complete protection against this tumor. The ability of interferon to "induce" class I gene expression may be an important modality in the treatment of a variety of spontaneous tumors that exhibit greatly reduced levels of class I antigens on their cell surface.
AuthorsH Hayashi, K Tanaka, F Jay, G Khoury, G Jay
JournalCell (Cell) Vol. 43 Issue 1 Pg. 263-7 (Nov 1985) ISSN: 0092-8674 [Print] United States
PMID4075396 (Publication Type: Journal Article)
Chemical References
  • H-2 Antigens
  • Interferon Type I
Topics
  • Adenoviruses, Human (physiology)
  • Animals
  • Cell Line
  • Cell Membrane (immunology)
  • Cell Transformation, Neoplastic
  • Cell Transformation, Viral
  • H-2 Antigens (genetics)
  • Interferon Type I (pharmacology)
  • Mice
  • Mice, Inbred C3H
  • Neoplasms, Experimental (etiology, immunology, pathology)
  • Transfection

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